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TigerPaw Pro Left Atrial Appendage Closure Device

FDA UDI

Class II (US FDA UDI)

by Datascope Corp.

Identity

Trade Name
TigerPaw Pro Left Atrial Appendage Closure Device FDA UDI
Generic Name
Open-surgery manual linear cutting stapler, single-use FDA UDI
Device Name
Left Atrial Appendage Closure Device 35mm - 7 pin FDA UDI
Model / Reference
35mm FDA UDI
Description
Left Atrial Appendage Closure Device 35mm - 7 pin FDA UDI

Identifiers

Catalog Number
750001099 FDA UDI
Primary DI / UDI-DI
10607567510996 FDA UDI
FDA Product Code
GDW FDA UDI
FTL FDA UDI
GMDN Term
Open-surgery manual linear cutting stapler, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4750 FDA UDI
878.3300 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

TigerPaw Pro Left Atrial Appendage Closure Device by Datascope Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Datascope Corp.

Sources (1)

  • FDA UDI 252f168f-b8b0-41e9-9cde-8c1ebf838e4b 35 fields · synced May 30, 2026